Clinical Data Programmer – Hybrid/Remote

Regulatory Toolkit; Maryland; Hybrid; USD 90,000 - 130,000; Full time

Job summary

Waters is seeking a Clinical Database Programmer to design, develop, implement, and maintain clinical databases and data management programming for clinical studies. You will collaborate across Data Management, Statistics, Clinical Operations, Medical Affairs, and IT to ensure high-quality, analysis-ready data.

You will lead end-to-end programming, build EDC databases, implement quality checks, and support database lock and audit readiness in a regulated environment.

Qualifications

• Bachelor's degree in a related field or equivalent experience
• Minimum 3 years of clinical database programming in pharma/biotech/CRO
• Experience supporting studies from database build through database lock
• Experience with Veeva CDMS or equivalent EDC platforms

Responsibilities

• Lead end-to-end clinical database programming for assigned studies.
• Design, build, configure, test, and maintain EDC databases per study specifications.
• Develop edit checks, derivations, form logic, and data quality controls.
• Create, validate, and maintain data transfer specifications and external data integrations.
• Support database lock activities and inspection readiness.

Skills

SQL

SAS

Veeva CDMS

EDC

Data lifecycle

Education

Bachelor's degree in Computer Science or Life Sciences

Tools

Veeva CDMS

SQL tooling

Job description

Waters is seeking a Clinical Database Programmer to design, develop, implement, and maintain clinical databases and data management programming for clinical studies. You will collaborate across Data Management, Statistics, Clinical Operations, Medical Affairs, and IT to ensure high-quality, analysis-ready data.

You will lead end-to-end programming, build EDC databases, implement quality checks, and support database lock and audit readiness in a regulated environment.